Listerine Antiseptic

Dosage form: mouthwash
Ingredients: Eucalyptol 0.92mg in 1mL, Menthol, Unspecified Form 0.42mg in 1mL, Methyl Salicylate 0.6mg in 1mL, Thymol 0.64mg in 1mL
Labeler: Johnson & Johnson Consumer Inc.
NDC code: 42002-401

Medically reviewed by Drugs.com. Last updated on Aug 30, 2024.

Listerine Antiseptic

Drug Facts

Active ingredients	Purposes
Eucalyptol 0.092% } Menthol 0.042% } Methyl salicylate 0.060% } Thymol 0.064% }	Antiplaque/antigingivitis

Uses

helps prevent and reduce:

plaque
gingivitis

Warnings

Do not use in children under 12 years of age

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

rinse full strength for 30 seconds with 20 ml (2/3 fluid ounce or 4 teaspoonfuls) morning and night
do not swallow

Other information

store at room temperature
cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

water, alcohol (26.9%), benzoic acid, poloxamer 407, sodium benzoate, caramel

Questions?

call 1-888-222-0182, weekdays

Dist: Johnson & Johnson Healthcare Products
Division of McNEIL-PPC, Inc.
Skillman, NJ 08558-9418 USA

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

LISTERINE®
ORIGINAL
ANTISEPTIC

Kills Germs that Cause
Bad Breath, Plaque & the
Gum Disease Gingivitis

ADA
Accepted
American
Dental
Association®

500 mL (1.05 Pt)

LISTERINE ANTISEPTIC
eucalyptol, menthol, methyl salicylate, and thymol mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:42002-401
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Eucalyptol (Eucalyptol)	Eucalyptol	0.92 mg in 1 mL
Menthol, Unspecified Form (Menthol, Unspecified Form)	Menthol, Unspecified Form	0.42 mg in 1 mL
Methyl Salicylate (SALICYLIC ACID)	Methyl Salicylate	0.6 mg in 1 mL
Thymol (Thymol)	Thymol	0.64 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Alcohol
Benzoic Acid
Poloxamer 407
Sodium Benzoate
Caramel

Packaging
#	Item Code	Package Description
1	NDC:42002-401-73	250 mL in 1 BOTTLE, PLASTIC
2	NDC:42002-401-72	500 mL in 1 BOTTLE, PLASTIC
3	NDC:42002-401-71	1000 mL in 1 BOTTLE, PLASTIC
4	NDC:42002-401-70	1500 mL in 1 BOTTLE, PLASTIC
5	NDC:42002-401-63	3700 mL in 1 BOTTLE, PLASTIC
6	NDC:42002-401-94	2 BOTTLE, PLASTIC in 1 PACKAGE
6	NDC:42002-401-70	1500 mL in 1 BOTTLE, PLASTIC
7	NDC:42002-401-95	95 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part356	03/01/2011	12/10/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 09/2020

Document Id: 5514d206-f86c-48c0-998f-0251118c10e1

Set id: 56f1e582-807c-43bb-b680-98e13852199f

Version: 3

Effective Time: 20200909

Johnson & Johnson Consumer Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

Listerine Antiseptic

Further information

See also:

Qulipta

Aimovig

Dupixent

Gemtesa

Ubrelvy

Nurtec ODT

Xeomin

Tazarotene topical

Topiramate

Dysport